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Ataxia v1.69 COQ5 Zornitza Stark Phenotypes for gene: COQ5 were changed from Coenzyme Q10 deficiency, primary 9, MIM#619028; Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability to Coenzyme Q10 deficiency, primary, 9 MIM#619028
Ataxia v1.68 COQ5 Zornitza Stark Publications for gene: COQ5 were set to 29044765
Ataxia v1.67 COQ5 Zornitza Stark Classified gene: COQ5 as Green List (high evidence)
Ataxia v1.67 COQ5 Zornitza Stark Gene: coq5 has been classified as Green List (High Evidence).
Ataxia v1.66 Zornitza Stark Added reviews for gene COQ5 from panel Mendeliome
Ataxia v1.65 Lucy Spencer Added reviews for gene COQ5 from panel Mendeliome
Ataxia v0.260 COQ5 Zornitza Stark Phenotypes for gene: COQ5 were changed from Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability to Coenzyme Q10 deficiency, primary 9, MIM#619028; Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability
Ataxia v0.259 COQ5 Zornitza Stark edited their review of gene: COQ5: Changed phenotypes: Coenzyme Q10 deficiency, primary 9, MIM#619028, Cerebellar ataxia, encephalopathy, generalized tonic-clonic seizures, intellectual disability
Ataxia v0.183 COQ5 Zornitza Stark Marked gene: COQ5 as ready
Ataxia v0.183 COQ5 Zornitza Stark Gene: coq5 has been classified as Red List (Low Evidence).
Ataxia v0.24 COQ5 Bryony Thompson gene: COQ5 was added
gene: COQ5 was added to Ataxia - paediatric_RMH. Sources: Expert list
Mode of inheritance for gene: COQ5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COQ5 were set to 29044765
Phenotypes for gene: COQ5 were set to Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability
Review for gene: COQ5 was set to RED
Added comment: Only one reported family, without functional assays linking the gene to ataxia.
Sources: Expert list